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A study on the central mechanism of paired associative stimulation in regulating individual mapping neural circuits related to balance function

A study on the central mechanism of paired associative stimulation in regulating individual mapping neural circuits related to balance function

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063501
Enrollment
Unknown
Registered
2022-09-08
Start date
2022-09-08
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stroke

Interventions

TMS group:paired associative stimulation
sham group:sham paired associative stimulation

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Part One: 1. Age >= 40 years old and 24. Part Two: 1. Onset of the first stroke; 2. Stroke recovery period, disease duration >= 6 months; 3. Age >= 40 years old and 24.

Exclusion criteria

Exclusion criteria: Part One: 1. The subjects had poor compliance and did not receive corresponding intervention according to the trial protocol; 2. The subjects refused to continue the subsequent intervention; 3. The subject quits voluntarily for unknown reasons; 4. After TMS intervention, the subject had TMS-related adverse events and refused to continue the treatment; 5. The subject has some comorbidities, complications, and special physiological changes, and is not suitable to continue to participate in this study; 6. The researcher considers it inappropriate to continue to participate in the study. Part Two: 1. There are contraindications of Mr, such as a pacemaker, a cardiac stent, claustrophobia, etc.; 2. There are contraindications to transcranial magnetic stimulation, such as cochlear implantation, history of epilepsy, metal implantation in vivo; 3. pregnant or lactating women; 4. non-right-handed hand; 5. Participated in or is participating in other clinical projects one month before enrollment; 6. Past month and current use of benzodiazepines, baclofen, and antidepressants.

Design outcomes

Primary

MeasureTime frame
functional reach test;

Secondary

MeasureTime frame
Berg Balance Scale;Modified Barthel Index,MBI;MRI;Technobody test;time-up and then go test;

Countries

China

Contacts

Public ContactWu Jiajia

Yueyang Integrated Chinese and Western Medicine Hospital affiliated to Shanghai University of Traditional Chinese Medicine

wujiajia@shutcm.edu.cn+86 15161769295

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026